{{Rsnum
|rsid=387906639
|Chromosome=5
|position=140674776
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HARS
|Gene_s=DND1,HARS
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=5
|CLNACC=RCV000022619.24
|CLNALLE=1
|CLNDBN=Usher syndrome, type 3B
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=CN121957:614504:231183:886
|CLNHGVS=NC_000005.9:g.140054361T>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=142810.0001
|Disease=Usher syndrome
|FwdALT=C
|FwdREF=A
|REF=T
|RSPOS=140054361
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906639
|GENEINFO=DND1:373863
|GENE_ID=373863
|GENE_NAME=DND1
}}